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Mephedrone and Nicotine: Oxidative Stress and Behavioral Interactions in Animal Models

The purpose of our experiment was to examine the influence of co-administration of nicotine and mephedrone on anxiety-like behaviors, cognitive processes and the nicotine-induced behavioral sensitization as well as processes connected with induction of oxidative stress in the brain of male Swiss mic...

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Autores principales: Budzynska, Barbara, Boguszewska-Czubara, Anna, Kruk-Slomka, Marta, Kurzepa, Jacek, Biala, Grazyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422847/
https://www.ncbi.nlm.nih.gov/pubmed/25862193
http://dx.doi.org/10.1007/s11064-015-1566-5
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author Budzynska, Barbara
Boguszewska-Czubara, Anna
Kruk-Slomka, Marta
Kurzepa, Jacek
Biala, Grazyna
author_facet Budzynska, Barbara
Boguszewska-Czubara, Anna
Kruk-Slomka, Marta
Kurzepa, Jacek
Biala, Grazyna
author_sort Budzynska, Barbara
collection PubMed
description The purpose of our experiment was to examine the influence of co-administration of nicotine and mephedrone on anxiety-like behaviors, cognitive processes and the nicotine-induced behavioral sensitization as well as processes connected with induction of oxidative stress in the brain of male Swiss mice. The results revealed that co-administration of subthreshold doses of mephedrone and nicotine (0.05 mg/kg each) exerted marked anxiogenic profile in the elevated plus maze and displayed pro-cognitive action in the passive avoidance paradigm (nicotine 0.05 mg/kg and mephedrone 2.5 mg/kg). Furthermore, one of the main findings of the present study was that mephedrone, administered alone at the dose not affecting locomotor activity of mice (1 mg/kg), enhanced the expression of nicotine-induced locomotor sensitization. Moreover, mephedrone administered with nicotine decreased general antioxidant status and catalase activity as well as antioxidant enzymes activity in the hippocampus and prefrontal cortex and increased concentration of malondialdehyde, an indicator of lipid peroxidation processes. Considering the likelihood that mephedrone is taken as a part of polydrug combination with nicotine, the effects of this combination on mammalian organisms have been confirmed in our study. Understanding the consequences of co-administration of psychoactive substances on the central nervous system and oxidative processes in the brain provide the important toxicological significance, and may be useful in polydrug intoxication treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11064-015-1566-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-44228472015-05-13 Mephedrone and Nicotine: Oxidative Stress and Behavioral Interactions in Animal Models Budzynska, Barbara Boguszewska-Czubara, Anna Kruk-Slomka, Marta Kurzepa, Jacek Biala, Grazyna Neurochem Res Original Paper The purpose of our experiment was to examine the influence of co-administration of nicotine and mephedrone on anxiety-like behaviors, cognitive processes and the nicotine-induced behavioral sensitization as well as processes connected with induction of oxidative stress in the brain of male Swiss mice. The results revealed that co-administration of subthreshold doses of mephedrone and nicotine (0.05 mg/kg each) exerted marked anxiogenic profile in the elevated plus maze and displayed pro-cognitive action in the passive avoidance paradigm (nicotine 0.05 mg/kg and mephedrone 2.5 mg/kg). Furthermore, one of the main findings of the present study was that mephedrone, administered alone at the dose not affecting locomotor activity of mice (1 mg/kg), enhanced the expression of nicotine-induced locomotor sensitization. Moreover, mephedrone administered with nicotine decreased general antioxidant status and catalase activity as well as antioxidant enzymes activity in the hippocampus and prefrontal cortex and increased concentration of malondialdehyde, an indicator of lipid peroxidation processes. Considering the likelihood that mephedrone is taken as a part of polydrug combination with nicotine, the effects of this combination on mammalian organisms have been confirmed in our study. Understanding the consequences of co-administration of psychoactive substances on the central nervous system and oxidative processes in the brain provide the important toxicological significance, and may be useful in polydrug intoxication treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11064-015-1566-5) contains supplementary material, which is available to authorized users. Springer US 2015-04-11 2015 /pmc/articles/PMC4422847/ /pubmed/25862193 http://dx.doi.org/10.1007/s11064-015-1566-5 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Budzynska, Barbara
Boguszewska-Czubara, Anna
Kruk-Slomka, Marta
Kurzepa, Jacek
Biala, Grazyna
Mephedrone and Nicotine: Oxidative Stress and Behavioral Interactions in Animal Models
title Mephedrone and Nicotine: Oxidative Stress and Behavioral Interactions in Animal Models
title_full Mephedrone and Nicotine: Oxidative Stress and Behavioral Interactions in Animal Models
title_fullStr Mephedrone and Nicotine: Oxidative Stress and Behavioral Interactions in Animal Models
title_full_unstemmed Mephedrone and Nicotine: Oxidative Stress and Behavioral Interactions in Animal Models
title_short Mephedrone and Nicotine: Oxidative Stress and Behavioral Interactions in Animal Models
title_sort mephedrone and nicotine: oxidative stress and behavioral interactions in animal models
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422847/
https://www.ncbi.nlm.nih.gov/pubmed/25862193
http://dx.doi.org/10.1007/s11064-015-1566-5
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